Development of a Rapid Detection Method for Yersinia pestis by Polymerase Chain Reaction.
- Author:
Ho Jung OH
;
Hong Ki MIN
;
Yeo Won SOHN
;
Jeong Hoon CHUN
;
Han Oh PARK
- Publication Type:Original Article
- MeSH:
DNA;
DNA Primers;
Enterobacteriaceae;
Korea;
Limit of Detection;
Plasminogen Activators;
Polymerase Chain Reaction*;
Stem Cells;
Yersinia pestis*;
Yersinia*
- From:Journal of the Korean Society for Microbiology
1999;34(4):373-383
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
A polymerase chain reaction (PCR) method for detection of the pathogenic Yersinia pestis from other Yersinia spp. was developed. Five Y. pestis strains, ninety-two other Yersinia species and twenty-four Enterobacteriaceae strains were collected in Korea and from other countries. Oligonucleotide primers were designed from pathogenic gene of antiphagocytic protein capsule gene (fra 1) and plasminogen activator gene (pla). The 428 bp DNA fragment was amplified from five Y. pestis which contained the fra I gene. No product was amplified from other Yersinia species and other strains of the Enterobacteriaceae. The 439 bp DNA fragment was amplified from three K pestis which contained the pla gene. No product was amplified from two Y. pestis, other Yersinia species and other strains of the Enterobacteriaceae. These showed that the designed primers were specific for detection of Y. pestis among other Yersinia species and Enterobacteriaceae strains. Amplification was successful whether the template was derived from purified DNA or from aliquots of boiled bacterial suspension. The detection limits were 100 pg of DNA and 100 colony forming units (CFU) for fra I and 100 pg DNA and 10 CFU for pla, respectively. Our results prove that the PCR method using specific primers for Y. pestis is a rapid and convenient procedure for routine clinical detection and identification of Y. pestis.
